Quality control analyst jobs in Chattanooga, TN

R&D Partners is seeking to hire a Quality Control Analyst in Holly Springs, NC. Your main responsibilities as a Quality Control Analyst: Performs testing and associated tasks without errors per applicable SOPs and protocols within Immunology/Biochemistry function. Properly documents test results in appropriates records and computer systems Complies with policies and procedures in order to maintain compliance with legal regulations, health and safety, and regulatory requirements as written. Participates in lean lab operation, 6S laboratory layout, preventive action & continuous improvement programs to reduce operating costs. Participates and performs in cross-training to support staff availability within QC department. What we are looking for in a Quality Control Analyst: Bachelor's degree (Biochemistry preferred, recent graduates ok) 1+ years of laboratory experience (ok if degree related) Knowledge of analytical methods and related instrumentation (ok if academic) Must already have or be willing to get a flu shot 1+ years of GMPs safety regulations and data integrity is preferred Why Choose R&D Partners? As an employee, you have access to a comprehensive benefits package including: Medical insurance - PPO, HMO & Dental & Vision insurance 401k plan Employee Assistance Program Long-term disability Weekly payroll Expense reimbursement Online timecard approval Pay Scale: $52,000 - $62,400 Dependent on Experience) R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies. R&D Partners is an equal-opportunity employer. If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page. R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - ******************************************* Desired Skills and Experience BS Biochemistry, or related. Knowledge of analytical methods and instrumentation, ELISA, BCA, SRID, SDS-PAGE

Title: Sterility Assurance Scientist Duration: 6 Month Contract (potential of extension) Responsibilities: The Sterility Assurance Scientist is a technical role that assists in development and implementation of the site's sterility assurance programs and provides technical guidance and expertise in environmental monitoring, contamination control, aseptic process simulations, gowning/aseptic techniques, and cleaning/sanitization strategies, including disinfectant efficacy. The principal role is a position that develops and implements a technical agenda and is responsible for providing technical leadership for the Parenteral Process Team. The principal role is also expected to serve as a mentor within the TSMS team and engage in upstream and external to site activities related to sterility assurance contamination control strategies are established. Key Objectives/Deliverables • (Associate/Senior) Ensure and provide oversight and technical guidance for sterility assurance programs at the manufacturing floor level. • Lead or provide technical oversight for Provide technical support for activities related to sterility assurance programs including but not limited to: • Airflow Pattern Testing • Environmental Monitoring Performance Qualifications • Aseptic Process Simulations • Cleaning, Sanitization, and Disinfection • Gowning within GMP Classified Areas • Aseptic Processing Techniques • Contamination Control • Assist in the development and implementation of processes and facility monitoring to ensure effective contamination control strategies are established. • (Senior) Lead or assist in the development and implementation of processes and facility monitoring to ensure effective contamination control strategies are established. • (Senior) Lead/assist with support and/or provide technical expertise for developing the site's contamination control strategy and cleaning and sanitization program/strategy, and disinfectant efficacy strategies. • (Senior) Lead/assist with support and/or provide technical expertise for the facility's cleanroom gowning and aseptic technique strategy/program. • (Principal) Knowledge in pharmaceutical Microbiology, related to microbiological media, microbiological enumeration techniques, and microorganism isolation and identification. • (Principal) Lead/provide technical oversight for one or both the Environmental Monitoring (EM) or Aseptic Process Simulation (APS) program: • (EM) Authoring EM Performance Qualifications (EM PQ) and overseeing the execution. • (EM) Evaluating EM data and authoring EM Trend Reports. • (EM) Assist with identifying facility environmental isolates and how to create and maintain environmental isolated cultures. • (APS) Authoring APS protocols and overseeing the execution. • (APS) Evaluating the APS data, including personnel qualifications, and authoring APS reports. • (APS) Assist with tracking and tending APS to ensure all regulatory requirements and Global Quality Standards are met for each manufacturing line/process. • Apply sterility assurance risk management to evaluate manufacturing processes and associated controls with respect to potential introduction of microbial, endotoxin, and particulate contamination. • Analyze microbial and manufacturing data to identify trends, process discrepancies, and opportunities for continuous improvements.• Lead or provide technical support for root cause investigations associated with sterility assurance programs. • Participate and/or provide technical sterility assurance support during internal and external audits. • Create, execute, review, and/or approve technical documents and change controls related to sterility assurance programs. • Work within cross-functional teams to implement TS/MS objective and deliver on business and quality objectives. Basic Qualifications: • Bachelor's or master's degree in microbiology, Biology, Biochemistry, Biochemical Engineering, Chemical Engineering, or other related scientific discipline. • Demonstrated understanding and relevant experience of scientific principles required for manufacturing parenteral drug products within operations, microbiology, environmental monitoring, sterility assurance, validation, technical services, and/or quality assurance associated cGMP pharmaceutical manufacturing. • (Senior) 2+ years in pharmaceutical manufacturing (Microbiology, TSMS, Sterility Assurance, or related dept). • (Principal) 5+ years in pharmaceutical manufacturing (Microbiology, TSMS, Sterility Assurance, or related dept). Additional Skills/Preferences: • Possess strong interpersonal skills to work cross-functionally within a team. • Possess strong self-management and organizational skills. • Possess strong oral and written communication skills for communicating to colleagues, management, and other departments. • Experience with data analysis and trending. • Ability to wear appropriate PPE and other safety related equipment or considerations in manufacturing warehouse, or laboratory areas. • Ability to gown into facility dedicated cleanroom attire, as required to perform job responsibilities. Additional Information: • Role is Monday through Friday based and will be phased from a project support role to a routine support role as the development facility and processes progress. Must be flexible in providing support to accommodate other inputs (production schedules, shutdowns, etc.). Occasional extended hours and / or off-hour work may be required. • Tasks may require repetitive motion and standing or walking for long periods of time. • Travel may be required during the project phase for training and implementation of sterility assurance programs. This is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the . For GMP purposes, the job description should be updated for significant changes. As always, you should consult with your supervisor regarding your actual job responsibilities and any related duties that may be required for the position.

Someone in this role will perform various scientific analyses to evaluate the quality of raw materials, in-process materials, and finished goods and ensure compliance with established standards. Conduct and validate various biological and chemical quality control (QC) assays Compile, interpret, and document statistical data from testing processes to either confirm compliance with established quality standards or identify deviations May be responsible for establishing specifications for conducting assays and writing standard operating procedures Requirements: Bachelors Degree Belcan is an equal opportunity employer. Your application and candidacy will not be considered based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.

HTI has an immediate opening for an experienced QC Chemist or Lab Analyst with an international manufacturing company at their Augusta, GA facility. This is an exciting opportunity to join a large, stable company that offers great benefits! Pay: $23 - $28/hour, depending on experience Working hours: Will train during normal working hours (Mon-Fri 8-5) and then go to a 12-hour rotating shift (a DuPont shift schedule, 7am-7pm/7pm-7am) Requirements: Must have Associate's or Bachelor's degree in Chemistry Must have 2+ years of recent experience as a QC Chemist or Lab Analyst with a manufacturing company, preferably in the pharmaceutical, food or chemical industry Experience with ICP, IC/HPLC and Titrators is strongly preferred Must have LIMS software and Microsoft Excel/Word/Outlook experience; SAP is preferred Must be open to working 12-hour rotating shifts Ability to add, subtract, multiply and divide in all units of measure, using whole numbers, common fractions and decimals; ability to compute rate, ratio, percent and basic statistical calculations Must currently be located in the Augusta, GA area and able to start a new position within 1-2 weeks after the interview Must be authorized to work in the U.S. without visa sponsorship (now or in the future) Summary: Responsible for the testing and disposition of raw material, in-process and finished product according to applicable procedures. Performs preparation of solutions and samples, calibration of analytical instruments, and interpretation of statistical analyses/results. Job Duties include: Performs analysis on bulk and packaged final products utilizing methods that comply with regulatory and other requirements (i.e., FCC, USP/NF, EP). Performs analysis on in-process samples to monitor and/or confirm that manufacturing specifications are being met. Participates in SQC charting of control samples; analyzing variations; and troubleshooting when necessary. Assures proper quality control of finished product for shipment and releases material in LIMS (Laboratory Information Management System) and SAP (Inventory Management System). Performs calibration, basic diagnostic, and troubleshooting procedures for laboratory instruments as needed. Generates Certificates of Analysis using the lab computer systems that comply with customer specifications. Assesses Out-of-Specifications (OOS) results, determines the impact on the product, and ensures timely resolution or corrective action as needed. Maintains laboratory supply inventory. Prepares samples along with necessary paperwork for shipment. Maintains historical records by implementing record keeping systems and filing documents. Maintains general housekeeping tasks to ensure a clean and organized work area; performs all activities in a safe and conscientious manner. Work Environment: The work environment requires normal safety precautions typical of such places as laboratories, offices, meeting and training rooms. Requires use of safe work practices with office equipment, avoidance of trips and falls, observance of fire regulations and traffic signals, etc. Generally, the work area is well lit, heated and ventilated. Environment may include work that requires special safety precautions such as working with irritant chemicals, around moving parts, carts or machines. Employee may be required to use protective clothing or gear such as masks, gowns, coats, safety shoes, boots, goggles, gloves, safety glasses or shields.

“Let goodness, fairness, and most importantly, love prevails in business; profits will inevitably follow.” - NK Chaudhary, founder Jaipur living is a socially conscious luxury brand with a passion for people, products, and design. A differentiated challenger brand, Jaipur Living is known for its beautiful rugs and textiles. Jaipur Living products can be found in the finest homes, and the company prides itself in providing only the highest quality products, a transparent and ethical supply chain, and distinctively thoughtful customer experience, with personalized support and custom offerings. Headquartered in a northwestern suburb of Atlanta, Jaipur Living designs, manufactures, and distributes rugs and other textiles through its extensive network of high-end interior designers and design firms, national retailers, and third-party e-commerce partners. The company continues to grow rapidly, experiencing double-digit annual growth every year for the past decade. This growth can be attributed to the care Jaipur Living puts not only in its customers but its employees as well. Employees at Jaipur Living are encouraged to collaborate, think independently, and stretch the creative process to develop new ways of marketing and distributing their products around the world. In August 2022, the company opened a new studio adjacent to its headquarters that, at over 17,000 square feet, functions as a communal space for design professionals to visit to experience Jaipur Living's products. The studio encapsulates not only our beautiful product but also the ways Jaipur makes lives beautiful through The Jaipur Rugs Foundation. What we do for our team members: Give competitive benefits and salaries Provide a friendly and professional work environment Maintain a modern, sleek facility, which complements our attitudes and desires Create opportunities for growth inside the company Give access to an on-site basketball court and gym complete with a yoga studio and showers Encourage employees to collaborate over an organic community garden Create employee events that build relationships and just have some fun! Our Values Empowerment • Inclusiveness • Responsibility • Progressive Learn more about our company story here: **************************************************** The Jaipur Rugs Foundation Since 2004, the Jaipur Rugs Foundation has worked to improve the lives of rug-weaving artisans in India. This is done through training, skills development, and social interventions. By focusing on the ideas and solutions that create social value, the Foundation supports the dignity and heritage of these traditional artisans, believing that healthy and sustainable communities are key to the survival of traditional rug weaving. Jaipur Living has made ethical and socially conscious global citizenship the foundation of its business. Through social initiatives and the Jaipur Rugs Foundation, the company supports a supplier ecosystem without a middleman of more than 40,000 artisans in 700 villages across India by providing them with a livable wage, access to health care, leadership education, and opportunities for personal growth and development. Combining time-honored techniques and of-the-moment trends, every Jaipur Living product is as ethically and responsibly made as it is beautiful. Learn more about the Jaipur Rugs Foundation here: *************************** Overview The Quality Control Technician will be a key member of the US Supply Chain team, collaborating and communicating with receiving, customer success, sales, inventory planning and other departments. The Quality Control Technician is responsible for supporting the execution of quality inspection processes and procedures by physical inspections. Ultimately the goal is to provide our customers with a high quality, beautiful product. This is the perfect role for someone who likes a combination of physical and mental work! What You Will Be Doing: Collaborate with customer success, sales, receiving and overseas teams to identify and correct quality issues. Maintain an ongoing list of problem vendors and problem items. Facilitate protocol for reviewing receipts of these items until all issues are resolved. Works under general supervision to perform routine product inspections related to labeling, packaging, color and size quality issues, following the relevant company's Standard Operating Procedures (SOP's) and methods. May be required to receive, sort, log issues into master qc log and prepare and apply labels Demonstrates good and safe work habits and enforces a clean working environment. May be required to archive, return, or dispose of inspected inventory as per the established procedure Will be required to operate warehouse machinery used for the purpose of re-stocking inspected inventory. Skills & Minimum Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. High School Diploma or equivalent is required Self-motivated and able to work independently when necessary Excellent relationship-building, and communication skills Strong organizational skills with attention to detail. Problem solving skills Proficiency with Microsoft Office Suite (Word, Excel) Physical Requirements: While performing the duties of this job, the employee is regularly required to sit; use hands to finger, handle, or feel; reach with hands and arms; and talk and hear. The employee must be able to stand, walk, bend, squat and crawl. The employee must frequently lift and/or move up to 20 pounds. Ability to react quickly to sounds. Work in an environment with varying temperatures. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. Must be able to take directional cues directly and indirectly. Employment at Jaipur is contingent on the completion of a criminal background check and a drug screen, with the results being negative. Jaipur employees are subject to pre-employment, post-injury, post-accident, reasonable suspicion, and random testing for illegal drug usage. Management retains the discretion to add or change the duties of this position at any time. Management retains the discretion to add or change the duties of this position at any time.

No Visa Sponsorship: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. The Senior Microbiologist is a critical technical resource in the QC Microbiology laboratory supporting the manufacturing of sterile injectable products. This position is responsible for independently performing and overseeing complex microbiological testing and environmental monitoring (EM) in compliance with cGMP, USP, FDA, and internal quality standards. This position is in a fast-paced, FDA regulated environment in the Pharmaceutical Industry. This role is mainly responsible for completing deviation investigations, OOS/OOT and CAPA development related to EM and microbiological testing. Maintains spreadsheets and databases to track and monitor department/company data, KPIs and metrics. Accountable for QC Microbiology inventory control including ordering materials, maintaining stock and resolving material complaints as needed. This role will serve as a Subject Matter Expert (SME) to provide guidance and support junior microbiologists. Train team members in aseptic technique, microbiological methods, EM sampling, and good documentation practices. Participate in the qualification of microbiology lab equipment. Identify and implement continuous improvement opportunities to optimize workflows in the quality control microbiology laboratory. OVERALL JOB RESPONSIBILITIES: Operational Excellence: Models the principles and behaviors of Glenmark and ensures personnel follow the company code of conduct. Communicate progress, status, and roadblocks as required. Drive projects, assignments, and complete presentations within timelines and budgets. Create and maintain relevant metrics for department/site. Spreadsheets and databases will be leveraged for departmental and company metrics, presentations, and data/testing tracking/verification. The Senior Microbiologist is responsible for keeping these sheets and databases up to date. Ability to perform routine testing of samples submitted to the laboratory as appropriate. Schedules and participates in cleaning, inventory, and maintenance tasks in the lab. Supports inventory management and ordering/stocking of all QC department laboratory supplies. Ensures laboratory equipment is in compliance with procedures and GLP requirements. Troubleshoots laboratory issues related to all instrumentation. Recommends potential corrective and/or preventive actions and implements these actions within the laboratory. Performs GMP review of test data to ensure that test results meet all specifications. Trends data and analyzes trends to proactively mitigate equipment and reagent performance issues. Verifies laboratory equipment and associated equipment logs to ensure proper operation Stakeholder: Preparation, review and approval of sampling matrix and hold time schedule Conducts and communicates results of lab investigations when test results fall outside pre-established specifications (OOS). Performs routine equipment maintenance. Performs maintenance of spare parts inventory, calibrations and supervises third party maintenance and repair when necessary. Establishes good working relation with contract laboratories. Supports in the development of methods transfer and validation, troubleshooting, cross validation, IQ/OQ/PQ protocols. Supports activities regarding audits of suppliers and contract labs in support of vendor certification program. Conducts statistical evaluation of the manufacturing and inspection process and training QC staff. Ensure that all equipment is calibrated. Responsible to develop and validate new test procedures Perform data analysis, compile data and generate reports for management review. Review lab test data and their integrity and adherence to SOPs and cGMP. Compliance: Maintain current knowledge of regulatory and industry standards, trends and advancements. Responsible for ensuring compliance to systems and procedures in the EM/Microbiology laboratory and cleanroom areas. And prepare the lab for internal and external audits. Support Continuous Improvement initiatives by providing support on updating SOPs, WIs, and OJT Complete and maintain certified investigator training requirements. Perform investigation of the quality events assigned using root cause analysis tools, maintain timelines for closure of investigations and identify/initiate CAPAs Complete and maintain status as a certified trainer Ensure Quality Systems are compliant with cGMPs and internal/external regulations and procedures Evaluates and assists in the implementation of new changes at the site, including providing training on an as needed basis Provide support to collect and prepare EMPQ reports, EM Trend reports, QMR board presentations with associated documentation. Performs regular self-audits of the Microbiology and EM laboratory areas (including storage areas) and assists/leads activities to address audit findings. Stakeholder: Works collaboratively with other department stakeholders to ensure the services provided to the site are developed, tested, and delivered according to established procedures and regulations. Innovation: Supports purchasing QC EM laboratory supplies. Makes sound, well considered decisions to make the most of available funds and resources. Monitors lab supply costs and looks for ways to work with suppliers to reduce consumables cost when appropriate. Consults with management, when appropriate, about laboratory supply variances. Demonstrates the ability to assess upcoming laboratory supply needs and prepare accordingly. Makes realistic and actionable plans to address supply chain issues. Maintains the QC department ordering system to reduce costs and waste due to expiry. Keeps current on physical and computerized tracking systems for materials and supplies. Safety: Appropriately utilizes PPE (Personal Protective Equipment) as required to perform routine and non-routine laboratory duties Education: KNOWLEDGE, SKILLS AND ABILITIES: Minimum BS/BA in Pharmaceutical Sciences, Chemistry, Biology Experience: Minimum of 3+ years in a pharmaceutical environment Strong organizational skills. Displays the ability to prioritize work and manage multiple tasks independently. Excellent written communication and technical writing skills. Clearly demonstrates competence in the selection and use of root cause analysis tools and techniques (e.g., 5 Whys, Pareto Analysis, 5M +E). Displays strong interpersonal skills and ability to work with all levels of an organization. Clearly expresses ideas (verbal and written) and demonstrates the ability to apply a quality mindset when completing Microbiology/EM laboratory tasks. Demonstrates the ability to read, understand, author, redline and execute standard operating procedures (SOPs). Displays ability to achieve Glenmark Monroe QE investigator certifications for product/process/testing/facility issues with product and non-product impact. Exhibits both analytical and problem-solving skills. Proven ability to problem solve/troubleshoot and provide solutions for laboratory issues. Able to assess safety and environmental risks to ensure laboratory tasks adhere to EHS management system. The ability to work independently and within team structure and on multiple projects, with flexibility to adapt to changing priorities is required. This candidate must be a technical expert and have excellent written and oral communication as well as interpersonal relationship skills. Ability to lift 30 lbs.' and work within different extreme temperature / humidity environments as encountered in the various Incubator conditions.

As a Quality Control Lab Technician, you will play a crucial role in maintaining the highest specifications in the industry for our organic products. You will work closely with the production team to perform live flour evaluations, monitor product quality throughout the production process, and ensure that our customers receive only the best organic flours. This position requires strong ability to catch and remember details, a sense of urgency, and a positive attitude. This job is full time and in person at the hours listed. No hybrid or remote options are available for this role. No visa sponsorship is available at this time. About Us Lindley Mills is an organic flour mill and mix manufacturer in Graham, North Carolina that was established in 1755. A long-standing family business, we mill the highest quality organic flours to give our customers a competitive advantage in every baked good. Whether we work with a national brand or our local farmer's market bakers, we provide the same high level of customer service and incredible products that cannot be found anywhere else. Our Super Sprout™ Sprouted Flour line is the gold standard for flavor, nutrition, and digestibility in the whole grain market. We are looking for team members who will grow with us and take on new challenges as we make these unique and innovative products accessible to everyone. Key Responsibilities - Conduct repeatable flour evaluation tests and monitor products against specification sheets. Learn to operate laboratory equipment and software, achieving accurate results. Performing routine cleaning and maintenance of lab equipment. - Perform lab tests using both sensory analysis and standard laboratory procedures. Document results and communicate them to management and production teams. - Maintain a clean and safe laboratory environment by adhering to Food Safety and GMP policies. Contribute to other cleaning duties outside of the lab as requested. - Assist the Quality Control Manager with lab and food safety initiatives, as well as other projects as needed, including packaging for e-commerce distribution. - Determine daily prioritization and preparation of incoming samples for testing. - Participate in cross-functional teams and contribute to research and development projects. - Maintain a stock of supplies and communicate needs to purchasing. Qualifications - Education: Bachelor's Degree - Experience: Minimum of 2 years in Quality Control or lab work. Experience in food service or baking is a plus. - Strong time management and organizational skills. - Excellent communication skills and ability to work collaboratively. - Very high attention to detail and a commitment to quality. - A sense of urgency and a proactive approach to problem-solving. Physical Requirements - Ability to stand for several hours a day (cushioned mats provided). - Must be able to safely lift at least 25 pounds. - All candidates must be able to safely work with and consume wheat products (no gluten or wheat sensitivities/intolerances/allergies). -Candidates must be able to hear, understand, and execute spoken directions throughout the day in a fast-paced production environment. -Candidates must be able to work while wearing personal PPE when required including hairnets, beard nets, earplugs, gloves, protective glasses, provided N95 masks, and lab coats. These are not all regularly worn in the lab, but may be worn during some duties. Hours and Benefits -Schedule: Monday to Friday, 7:30 AM - 4:30 PM. -Breaks: Two 15-minute breaks and a 1-hour lunch typically from 12 PM to 1 PM although may flex slightly with production needs. -Overtime: Opportunities available, but rarely required for lab personnel. -Benefits - Health insurance - SIMPLE IRA Retirement plan with company match - Paid vacation and holidays - Performance bonuses, raises, and promotional opportunities - Competitive pay commensurate with experience and contributions to the team. Career Growth Opportunities 1. Hands on Training that allows practice with oversight from an experienced lab technician. This will include grain and flour knowledge, equipment training, and review of written protocols for lab duties. 2. Budget for continuing education training courses or food safety certifications after tenure is achieved. 3. Mentorship from experienced food safety professionals who have over 30 years of organic audits, decades of Kosher audits, and 15+ years of BRC audits most recently maintaining AA or AA+ rated status over the last 5+ years. 4. Opportunity for internal advancement. 5. Work life balance: 40-hour work weeks with regular schedule. Nights and weekends rarely necessary unless prepping for a major audit. Paid vacation, paid holidays, SIMPLE IRA Retirement Plan with company match, Health Insurance. 6. Beautiful, rural location that's still within 30-45 minutes of Burlington, Chapel Hill, Siler City, Pittsboro, Graham, Greensboro, and Durham. 7. Company culture based on merit and contribution regardless any other factor. We want the best ideas put into practice no matter where they come from and we are listening! Commitment to Diversity: Lindley Mills is an equal opportunity employer and does not discriminate based on protected characteristics such as: age, race, color, sex, national origin, disability, or religion. We believe in a merit-based work and reward system. We know that different experiences and viewpoints, when brought together constructively as a team, can improve business outcomes and product or service offerings for our customers. If this position caught your eye, check out our other posted roles and send us your resume and cover letter explaining why you think you would be a great candidate for this role. For best consideration include the job title and source where you found this position in the subject line of your email to ************************. Already a candidate? Please connect with your recruiter to discuss this opportunity.

Who are we? At Scalian, we are a leading multinational engineering consulting firm with 5,500 specialists and over 30 years of experience. We are specialized in Industrial Performance (Quality Assurance, Supply Chain, and Project Management) and Digital Systems (IT & Software and Systems Engineering). Our expertise serves various technological sectors such as the aerospace, defense, rail, and energy industries while providing distinctive support to their development and operations. Are you an experienced Quality Controller? If your answer is yes, it's your lucky day as we are looking for a dynamic and talented person to join our team in the US! What will your role be? As a Quality Controller, you'll play a vital role in ensuring products, components, and processes conform to established quality and regulatory standards. This position is heavily focused on hands-on product control work, documentation accuracy, and clear communication across teams. You will be responsible for ensuring detailed inspections, identifying nonconformities, issuing corrective action reports, and ensuring compliance with technical requirements. Activities: Identify, document, and classify nonconformities; generate Nonconformance Reports (NCRs) with clear, detailed descriptions Create and issue Corrective Action Requests (CARs), ensuring problem statements are accurate and actionable Collaborate with internal teams to support root cause analysis and ensure corrective actions are implemented effectively Maintain accurate inspection records, traceability documentation, and quality logs Communicate inspection results, quality issues, and required corrective actions clearly to production, engineering, and supplier teams Verify compliance with customer specifications, regulatory requirements, and internal quality procedures Support audits and process verification activities as needed Escalate significant quality risks promptly and participate in establishing containment measures Be adaptable to additional inspection-related tasks or changes driven by business needs What skills and qualifications are we looking for? Associate degree or certification required, preferably in Quality Assurance, Manufacturing, or a technical field Inspection Authorization (IA) holder strongly preferred Minimum of 3 years' experience in Quality in a manufacturing, aerospace, or similar regulated industry Strong understanding of inspection methods, measurement tools, and quality documentation practices Ability to write clear, accurate NCRs and corrective action documentation Excellent communication skills with the ability to convey inspection findings and requirements effectively Flexibility, strong attention to detail, and initiative to drive effective quality solutions Work environment typically quiet with occasional moderate noise levels Why join us? To acquire experience in different critical industries and projects while working for the same company; To have a competitive salary and a great benefits package To access trainings that focus on expanding your knowledge while staying up to date with cutting edge technologies and best practices; To have a clear career development plan that suits your goals; To have the possibility of working abroad through our mobility program thanks to our international presence; To join a dynamic, specialized and fast-growing group where communication is key and where every team member is valued. To be part of a team where having fun is essential.

Johnson Service Group (JSG) is a nationally recognized professional staffing and recruiting firm that is looking for an experienced Environmental Laboratory Analyst to fill a contract assignment in Atlanta, Georgia. Job Title: Environmental Laboratory Analyst Work Location: Atlanta, GA 30339 Requirements LABORATORY TECHNICIAN Education Some college preferred (Science based studies preferred) PPE Equipment Knowledge & Skills Safety glasses, long pants, closed toe shoes, and neoprene gloves (as needed). Experience: Experience in a National Environmental Laboratory Accreditation Conference (NELAC) or highly regulated laboratory environment preferred. Experience in the Sample Receiving department of a high-volume laboratory. Wet chemistry experience preferred (pH, ammonia, alkalinity, turbidity, etc…) Handling and preparing environmental samples for analysis according to EPA, ASTM, or other protocols. Key Responsibilities: Work safely, identify and implement corrective actions for unsafe working conditions. Receive and log-in samples to our Laboratory Information Management System (LIMS) for analysis. Prepare inorganic and organic samples for analysis using a variety of laboratory instrumentation and analytical methodology. (EPA and ASTM), as needed. This can include, but isn't limited to preserving samples with acid, etc… Order and maintain the appropriate number of sample bottles and/or containers for environmental sampling. Perform routine laboratory housekeeping and assist Laboratory Analysts on an as needed basis. Perform miscellaneous administrative duties such as supply inventory and ordering, organization, peer review of data entry, etc… Support customers with filling sample container orders, coordinate sample sub-outs, contact customers as needed to ensure accuracy and clarity with requested analysis. Abilities: Must have excellent Communication and Interpersonal Skills. Ability to interface with a variety of internal/external work groups and plant personnel. - Must have computer proficiency utilizing Microsoft Office suite (Excel, Word, etc…), instrument and data management software. Understanding of OSHA laboratory safety requirements under 40 CFR 1910. This position requires personal protective equipment This position may require some bending, lifting, climbing, prolonged sitting, prolonged walking, walking on gravel or crawling when necessary. JSG offers medical, dental, vision, life insurance options, short-term disability, 401(k), weekly pay, and more. Johnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, marital status, protected veteran status, or any other characteristic protected by law. #D650

Fully Onsite - Standard hours - Up to 5 days per month may require shift flexibility. We are seeking a highly motivated and experienced Senior Associate in Quality Control (QC) Chemistry to support the startup and operational readiness of our QC laboratory. Working with minimal supervision, this individual will lead and contribute to critical activities including system qualifications, method transfers, and laboratory operations in a GMP-regulated environment. Key Responsibilities: • Collaborate cross-functionally with site teams to implement work order and preventative maintenance systems for laboratory equipment. • Review and contribute to validation documentation to support onboarding of equipment and computerized systems. • Draft, revise, and review technical and quality documentation such as SOPs, test methods, technical assessments, validation reports, trend reports, and safety evaluations. • Assist in the procurement of laboratory consumables and critical reagents required for startup activities. • Coordinate and execute training and method transfer activities for instruments including HPLC, UPLC, TOC, and other chemistry-based platforms. • Actively participate in audits, quality initiatives, and cross-functional projects with site or global impact. • Provide routine operational support during weekends and public holidays as required. Preferred Qualifications: • Bachelor's degree or higher in Chemistry, Biochemistry, Chemical Engineering, Physics, or a related scientific discipline. • Minimum of 4 years of relevant laboratory experience in a GMP pharmaceutical or biopharmaceutical manufacturing environment, with a strong background in analytical testing. • Proficient in analytical laboratory techniques and instrumentation. • Familiarity with laboratory systems such as LIMS and LMES/CIMS. • Demonstrated understanding of industry regulations, data integrity, and compliance standards. • Strong technical writing, documentation, and communication skills. • Experience with method and equipment validation, including verification, transfer, and change control. • Excellent interpersonal skills with the ability to collaborate across teams and adapt to varying communication styles. Top 3 Skills: Must be flexible Must have a chemistry background Nice to have: cGMP knowledge Day to Day Responsibilities: Daily responsibilities include routine sample testing, method transfers, and method validations based on laboratory activities.

We are hiring Chemist - I. Please let me know if you are interested or anyone who might be interested. Client: Major Pharmaceutical Manufacturing Client Chemist - I Duration: 6+ months on W2 ONLY Pay Rate: $24.00-$25.00/ Hr ***LOOKING FOR ENTRY LEVEL GRADUATES WITH CHEMISTRY BACKGROUND*** __________________________________________________________________ DESCRIPTION: Work Location: Wilson - NC Onsite Job Summary Performs a variety of chemical analyses and GMP review in accordance with cGMP, GLP, DEA and company policies and procedures. Primary Responsibilities Perform routine testing (dissolution, assay/degradant, content uniformity and ID) of drug products in a cGMP laboratory. Complete all assigned testing in a timely and organized manner in accordance with cGMP, GLP, DEA and company policies and procedures. Enter data into laboratory information system and accurately document all necessary and relevant information in a clear concise manner as per cGMPs. Operate and maintain all analytical instrumentation and equipment as per established procedures; perform basic troubleshooting. Communicate openly within the group to provide and gather information, to optimize the use of resources and to optimize efficiency. Aid other group members as required. Ensure that equipment and working areas are maintained with good safety and housekeeping practices. Re-stock chemicals and consumables used in analysis. Performs other related assignments and duties as required and assigned. Education and Experience Requirements The incumbent must have a BA or BS degree in Chemistry or closely related science. Minimum of 1-year relevant experience preferred. Necessary Knowledge, Skills, and Abilities Understanding of analytical technology (HPLC, GC, Dissolution, Automation, or Spectroscopy - UV/Vis, NIR, IR, or AA/AE). Relevant experience may include academic and/or industry experience and is measured based on the quality and quantity of the experience as it relates to the requirements of the position. Regards Vishnu Das Natesan ********************

Accentuate Staffing is assisting a growing food and beverage manufacturer in the Garner area who is hiring a Quality Control Supervisor to join their team. This is a direct hire opportunity offering excellent benefits. Responsibilities: Oversee daily activities for Quality Control Technicians and Syrup Blenders Lead, train, and support QC Technicians and Syrup Blenders to ensure smooth daily operations. Oversee product testing, ingredient checks, and syrup quality verification to keep everything in spec. Maintain proper calibration of lab equipment and ensure all testing processes follow internal and regulatory standards. Manage inventory accuracy for concentrates, raw materials, and finished syrups. Keep detailed documentation and ensure all records meet audit readiness standards. Assist with hands-on lab or blending tasks as needed to keep production on track. Serve as the department lead in the absence of the Quality Control Manager. Lead quality oversight on the floor and will step in to support the team when needed Take on additional projects and responsibilities that support QC and production initiatives. Requirements: High School diploma or equivalent required; Associate's degree in a science-related field preferred. Background in science (chemistry strongly preferred). Previous experience in a supervisory role-ideally within a manufacturing, production, or lab environment. Working knowledge of GLPs, GMPs, and chemical safety. Strong communication skills and the ability to train, coach, and motivate a team. Proficiency with Microsoft Excel and Word. Accurate with documentation and attention to detail. Ability to work in a collaborative, team-oriented setting. Willingness to complete Quality Leadership Training and forklift/PIT certification. Flexibility to work the hours required to support operations.

Randstad (Recruiting for a Top Global Client) | Thompsons' Station, TN (Onsite) Role Details Job Title: Microbiology Analyst Duration: 6-month contract (Temp, with potential for full-time conversion Pay: 27.00 per hour Schedule: Must be able to work the required schedule: Tuesday-Saturday, 8:30 AM-5:00 PM. Inability to work weekends is a deal breaker. The Opportunity: What You'll Do You will be a key member of a 10-person lab team, contributing to critical product hold and release testing. Your main focus in the first 90 days will be completing training on sample preparation and petrifilm methods. Perform critical testing to ensure product quality and compliance. Work closely with other analysts and the line manager. Be a reliable, positive, and collaborative team player. Required Qualifications (Deal Breakers) Candidates who cannot meet these mandatory requirements will be automatically disqualified: Education: Associate of Science or Bachelor of Science in Biology, Chemistry, or a related field. Experience: 1-2 years in a laboratory environment. Physical: Must be able to lift 30 lbs. Preferred Skills That Will Make You Stand Out We're looking for someone with practical and theoretical knowledge of lab science: Microbiology Expertise: Experienced in PCR technologies, cultural plating methods, petrifilm use, and anaerobic plating methods. Quality Systems: Practical and theoretical knowledge of ISO 17025. Lab Operations: Knowledge of aseptic technique and cross-contamination management/mitigation in laboratories. Technical Tools: Experience and skill in using computers, spreadsheets (Excel), Word, ELN, and laboratory information management systems (LIMS). Soft Skills: Must be a strong communicator, detail oriented, a self-starter, and comfortable with ambiguity and change.

Work Schedule Rotating schedule from 7pm - 7am Job Description Join the Thermo Fisher Scientific team to contribute to global impact through meaningful work. Support our Mission daily to empower customers in creating a healthier, cleaner, and safer world. Location/Division Specific Information: Within the Pharma Services Group (PSG), the High Point, NC location specializes in gelatin-based drug delivery dosage forms (softgels). Our expertise lies in the development and production of various softgel technologies. How Will You Make an Impact? The Formulation Technician II will be responsible for operating an encapsulating machine to produce products from pre-mixed ingredients, ensuring accurate temperatures, machine settings, equipment set-ups, in-process measurements, and quality product. A Day in the Life: Manufacture simple, bulk products Observe machine operation, adjust as needed, take samples of product, and perform in-process testing Assist Set-Up person to set up machine, empty basket, clean and prepare machine for changeover, and assist with the actual changeover Assist with cleanup and other encapsulation duties as needed Operate inline printing equipment Education: High school diploma or equivalent experience required. Experience: Necessary: At least 1 year of professional experience in a manufacturing, operations, production, or lab environment or a relevant field Desired: Background in a cGMP setting Knowledge, Skills, Abilities: Excellent verbal and written skills Ability to interpret data, perform basic calculations, and troubleshoot Ability to work a 12-hour shift in a 24-hour, 7 day per week operation Meet DEA security clearance requirements if requested Must have the flexibility to work additional hours when needed Physical Requirements / Work Environment: Must have the ability to regularly lift, push, pull, or transport items weighing up to 50 pounds Adherence to all GMP Safety Standards Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed Loud noises (equipment/machinery) Some degree of PPE required (safety glasses, gowning, gloves, lab coat, ear plugs, etc.) Standing for full shift Working at heights What We Offer Compensation: Competitive hourly pay rate Additional shift differential for night shift positions Annual performance-based bonus Annual merit performance-based increase Excellent Benefits! Medical, Dental, & Vision benefits effective Day 1 Paid Time Off & Designated Paid Holidays Retirement Savings Plan Tuition Reimbursement Employee Referral Bonus Career Advancement Opportunities

What we offer Explore a world of opportunities with us. Look ahead with us and help shape innovative solutions to make our world more sustainable and life healthier, more vibrant and more comfortable. At Evonik, you have the chance to explore, thrive, and grow alongside 33,000 colleagues. Among attractive career paths and high-quality development programs, we not only offer performance-based remuneration and occupational health benefits but also hybrid and flexible working environments with #SmartWork. Bring your fresh perspective, develop your strengths, break out your mold, and find a career that fits your dreams with us. Click on the link below to learn what our employees have to say about Evonik: ************************************************** This position is responsible for conducting routine microbiological testing, documentation, and data analysis, of utilities, raw materials, facilities and equipment. Additionally, the microbiology technician will be responsible for upkeep of the laboratory, laboratory supplies, and other various routine laboratory tasks. Responsibilites: Has a sound understanding of the skills required to perform the following routine activities: Environmental Monitoring - Monitoring of Classified Areas using a) active/passive air sampling methods and RODAC/swab surface sampling methods for the detection of bacteria and fungi; and b) CliMet air sampling methods for the detection of Total Particulates; trending of this data to detect anomalies, and characterize the transient and resident microflora. Utilities -Testing of a) city water for total microbial count and the absence of enteric organisms; b) pre-treat water, clean steam and Water for Injection for total microbial count and presence of endotoxins; and c) nitrogen and process air for total microbial count and total particulates. Utilizes classical microbiological methods for the identification of microorganisms. Perform validation activities such as biological indictor recovery, bioburden rinse/swab, endotoxin rinse and endotoxin challenge vial testing. Data analysis and entry into software systems such as Microbiology Information Management Systems (MIMS). GMP Documentation - Document test results and conclusions in a GMP manner. Ensure test forms are complete before submission for approval. Performs responsibilities in compliance with Evonik quality systems. Adheres to all company safety, health and environmental policies, procedures and directives. Conducts all laboratory activities in a safe manner by use of MSDS to establish chemical hazards, observes the appropriate laboratory procedures and reports all incidents that could threaten the safety of laboratory personnel Requirements: Bachelor's degree in microbiology, biological sciences, or related field of study Minimum 1 yr. experience in a clinical, academic, or industrial/pharmaceutical microbiology laboratories. Experience in microbiological assays and testing. Desired experience in environmental monitoring and trending. Desired experience in the testing of utilities. Excellent written and verbal communication skills. Excellent organizational and leadership skills. Proficiency in Good Laboratory Practices (GLPs) and Good Manufacturing Practices (GMP). Excellent computer skills including experience with spreadsheets and databases. Ability to use a respirator. Ability to work with microorganisms and hot liquids. The Evonik Group adopts an Equal Employment Opportunity (EEO) approach. Candidates are assessed based on their educational qualifications, experience, job competencies and potential and shall not be discriminated against on the basis of race, ethnicity, age, gender, religion, nationality, disability or sexual orientation or other classifications protected by local, state, or provincial regulations. Your Application To ensure that your application is proceeded as quickly as possible and to protect the environment, please apply online via our careers portal. Further information about Evonik as Employer can be found at *************************** Please address your application to the Talent Acquisition Manager, stating your earliest possible starting date and your salary expectations. Your Talent Acquisition Manager: Kelvin Seals [C] Company is Evonik Corporation

Job Title: Microbiology Lab TechnicianJob Description A leading global pharmaceutical manufacturer specializing in diabetes-related products is seeking a Microbiology Lab Technician for their Quality Control Laboratory. This role involves assisting with daily operations of samples originating from three manufacturing plants and contract manufacturing partners. The technician will follow standard operating procedures and Good Manufacturing Practice (GMP) guidelines, conducting bioburden and other microbial tests as needed. Cross-training will be provided to support media preparation for testing, manufacturing, and other parts of the plant. Responsibilities + Conduct bioburden and other microbial testing in accordance with standard operating procedures and GMP guidelines. + Assist with the day-to-day operations of samples from multiple manufacturing plants and partners. + Support media preparation for testing and manufacturing processes. + Follow lab safety protocols and ensure compliance with quality control standards. + Read and interpret standard operating procedures (SOPs). Essential Skills + Proficiency in microbiology and aseptic techniques. + Experience in laboratory settings, either from academia or industry. + Familiarity with lab safety practices. + Ability to read and understand SOPs. + Experience with microbiology testing such as endotoxin or bioburden in a pharmaceutical lab. + Previous experience with GMP and quality control. Additional Skills & Qualifications + Previous industry experience in a Quality Control lab is a plus. Work Environment The position requires working first shift hours, Monday to Friday, on-site, with one weekend per month. Flexibility for potential weekend or second shift work may be needed, and candidates should express their comfort level with these shifts. Job Type & Location This is a Contract position based out of Clayton, NC. Pay and Benefits The pay range for this position is $30.99 - $30.99/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Clayton,NC. Application Deadline This position is anticipated to close on Dec 15, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Job Description Follow specific work instructions to meticulously inspect products for defects. Separate and identify good parts from those with imperfections. Label containers appropriately and mark defective parts as needed. Document and record data of checked parts daily, maintaining accurate records. Report any defects or concerns directly to the supervisor. Work collaboratively with clients and discuss quality findings when necessary. Qualifications: Excellent attendance and punctuality. Motivation to work efficiently and effectively. Must wear steel-toed shoes for safety. A great attitude and the ability to work well with others. Previous experience in quality inspection is beneficial but not required.

Job Description Move into a job designed for you! Join our team and be a part of the Natco family. As a fourth-generation family-run business, Natco Home is one of the largest and most respected privately owned home furnishings companies in North America. At Natco, surpassing our customers' expectations in quality, service, and value is over a 100-year tradition. A commitment to innovation is woven into our future. An inspired career path awaits. Come see for yourself, there is no place like Natco Home. What we need: The Quality Control Inspector ensures that all products meet established quality standards before leaving the production facility. This role involves inspecting materials, components, finished goods, identifying defects, and working closely with production teams to maintain compliance with company and regulatory requirements. What you'll do: Perform inspections on raw materials, in-process components, and finished products according to quality standards and specifications Document inspection results and maintain accurate records in compliance with company policies Identify and report defects or non-conformances to appropriate personnel Collaborate with production teams to resolve quality issues and implement corrective actions Ensure compliance with safety and regulatory standards throughout the inspection process Assist in continuous improvement initiatives to enhance product quality and reduce defects What you'll have: High School Diploma or equivalent Minimum of 1-3 years in quality control or manufacturing environment Expert-level computer literacy What you're good at: Strong digital and technology orientation Attention to Detail: Strong ability to detect defects and ensure compliance with standard Problem-Solving: Capable of identifying root causes and recommending corrective actions Communication: Clear verbal and written communication for reporting and collaboration Computer Literacy: Must be proficient in using computers for data entry, quality reporting, and basic software applications (e.g., Microsoft Excel, Word, and quality management systems) Time Management: Ability to prioritize tasks and meet inspection deadlines Teamwork: Works effectively with production and engineering teams to maintain quality standards APPLY TODAY! To be considered, please complete an online application. Come Home to Natco. Natco is pleased to offer comprehensive employee benefits to protect your health, support your family, and enhance your lifestyle. Our Benefits Package Features: Paid Time Off & Paid Holidays Medical, Dental, and Vision Health Reimbursement Account (HRA) Health Savings Account (HSA) Flexible Spending Account (FSA) Employer Paid Life Insurance 401(k) Retirement Plan with Company Match Natco Home, a fourth-generation family-owned business, proudly carries a legacy as one of the most respected and trusted names in the home furnishings industry. Established in 1917 in Rhode Island, Natco is one of the largest privately owned home furnishings companies in North America, with a robust distribution network spanning across the continent. Serving as a comprehensive home fashion resource, the Natco Home Group's exceptional product line-up of rugs, vinyl flooring, curtains, window treatments, and home décor products are available through major mass merchandisers, home centers, department stores, and clubs, not only in the United States, Canada, and Mexico but also in various other regions around the world. With a rich history in consumer goods manufacturing and a strong commitment to eco-friendly materials, Natco continues to adapt its product offerings to remain aligned with ever-evolving customer demands and market trends. Committed to innovation, Natco continues to venture into new product lines, solidifying its position as a leader in the industry. Natco is an Equal Opportunity Employer committed to an inclusive workplace.

Job Title: Lab Technician (Microbiology) Duration: 06+ Months Schedule: Thursday - Sunday 6 AM to 4: 30 PM or 01: 30 PM to 12: 00 AM (0600 - 1630 or 1330 to 0000) Recommended experience : 0-3 years for Associate level, 4-7 years Intermediate level, and 8+ for Senior level hires OBJECTIVES : Conducts and performs a wide range of biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods and may include environmental monitoring programs. Position may be applicable to QC Analytical or Microbiological testing, Compliance, QCMIS, or Laboratory Operations. Job Function and Description Identified responsibilities include : Collect samples from manufacturing areas to evaluate environmental classification or critical utility integrity. Conduct critical biological, chemical and physical analyses such as raw materials, initial, in-process and final products, and samples collected from environmental monitoring programs at the company manufacturing facilities, etc. Use sophisticated laboratory instrumentation and computer systems to collect and record data (such as LIMS system). Perform assays requiring precise analytical skills and understanding of biology and chemistry principles. Complete all testing, including special project/protocol testing in a timely and appropriate manner. Initiate and obtain applicable approval for test requests. May maintain inventory/supplies necessary to conduct routine testing. Follow continuous improvement practices (QLP, 5S, LEAN, etc.) Performs equipment maintenance and calibrations as required. Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations. Perform release functions in LIMS or other computerized systems. May perform other duties as assigned. Education and Experience Requirements Typically requires bachelor's degree in chemistry, biological science, or other related technical field. Some related work experience preferred. Microbiology: Environment monitoring, critical utility sampling, endotoxin testing, bioburden for raw materials and in process, process samples, microbial identification and final product sterility testing.